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Limited DNA Repair Gene Repertoire in Ascomycete Yeast Revealed by Comparative Genomics
Ascomycota is the largest phylogenetic group of fungi that includes species important to human health and wellbeing. DNA repair is important for fungal survival and genome evolution. Here, we describe a detailed comparative genomic analysis of DNA repair genes in Ascomycota. We determined the DNA re...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145719/ https://www.ncbi.nlm.nih.gov/pubmed/31693105 http://dx.doi.org/10.1093/gbe/evz242 |
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author | Milo, Shira Harari-Misgav, Reut Hazkani-Covo, Einat Covo, Shay |
author_facet | Milo, Shira Harari-Misgav, Reut Hazkani-Covo, Einat Covo, Shay |
author_sort | Milo, Shira |
collection | PubMed |
description | Ascomycota is the largest phylogenetic group of fungi that includes species important to human health and wellbeing. DNA repair is important for fungal survival and genome evolution. Here, we describe a detailed comparative genomic analysis of DNA repair genes in Ascomycota. We determined the DNA repair gene repertoire in Taphrinomycotina, Saccharomycotina, Leotiomycetes, Sordariomycetes, Dothideomycetes, and Eurotiomycetes. The subphyla of yeasts, Saccharomycotina and Taphrinomycotina, have a smaller DNA repair gene repertoire comparing to Pezizomycotina. Some genes were absent from most, if not all, yeast species. To study the conservation of these genes in Pezizomycotina, we used the Gain Loss Mapping Engine algorithm that provides the expectations of gain or loss of genes given the tree topology. Genes that were absent from most of the species of Taphrinomycotina or Saccharomycotina showed lower conservation in Pezizomycotina. This suggests that the absence of some DNA repair in yeasts is not random; genes with a tendency to be lost in other classes are missing. We ranked the conservation of DNA repair genes in Ascomycota. We found that Rad51 and its paralogs were less conserved than other recombinational proteins, suggesting that there is a redundancy between Rad51 and its paralogs, at least in some species. Finally, based on the repertoire of UV repair genes, we found conditions that differentially kill the wine pathogen Brettanomyces bruxellensis and not Saccharomyces cerevisiae. In summary, our analysis provides testable hypotheses to the role of DNA repair proteins in the genome evolution of Ascomycota. |
format | Online Article Text |
id | pubmed-7145719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71457192020-04-13 Limited DNA Repair Gene Repertoire in Ascomycete Yeast Revealed by Comparative Genomics Milo, Shira Harari-Misgav, Reut Hazkani-Covo, Einat Covo, Shay Genome Biol Evol Research Article Ascomycota is the largest phylogenetic group of fungi that includes species important to human health and wellbeing. DNA repair is important for fungal survival and genome evolution. Here, we describe a detailed comparative genomic analysis of DNA repair genes in Ascomycota. We determined the DNA repair gene repertoire in Taphrinomycotina, Saccharomycotina, Leotiomycetes, Sordariomycetes, Dothideomycetes, and Eurotiomycetes. The subphyla of yeasts, Saccharomycotina and Taphrinomycotina, have a smaller DNA repair gene repertoire comparing to Pezizomycotina. Some genes were absent from most, if not all, yeast species. To study the conservation of these genes in Pezizomycotina, we used the Gain Loss Mapping Engine algorithm that provides the expectations of gain or loss of genes given the tree topology. Genes that were absent from most of the species of Taphrinomycotina or Saccharomycotina showed lower conservation in Pezizomycotina. This suggests that the absence of some DNA repair in yeasts is not random; genes with a tendency to be lost in other classes are missing. We ranked the conservation of DNA repair genes in Ascomycota. We found that Rad51 and its paralogs were less conserved than other recombinational proteins, suggesting that there is a redundancy between Rad51 and its paralogs, at least in some species. Finally, based on the repertoire of UV repair genes, we found conditions that differentially kill the wine pathogen Brettanomyces bruxellensis and not Saccharomyces cerevisiae. In summary, our analysis provides testable hypotheses to the role of DNA repair proteins in the genome evolution of Ascomycota. Oxford University Press 2019-11-06 /pmc/articles/PMC7145719/ /pubmed/31693105 http://dx.doi.org/10.1093/gbe/evz242 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Milo, Shira Harari-Misgav, Reut Hazkani-Covo, Einat Covo, Shay Limited DNA Repair Gene Repertoire in Ascomycete Yeast Revealed by Comparative Genomics |
title | Limited DNA Repair Gene Repertoire in Ascomycete Yeast Revealed by Comparative Genomics |
title_full | Limited DNA Repair Gene Repertoire in Ascomycete Yeast Revealed by Comparative Genomics |
title_fullStr | Limited DNA Repair Gene Repertoire in Ascomycete Yeast Revealed by Comparative Genomics |
title_full_unstemmed | Limited DNA Repair Gene Repertoire in Ascomycete Yeast Revealed by Comparative Genomics |
title_short | Limited DNA Repair Gene Repertoire in Ascomycete Yeast Revealed by Comparative Genomics |
title_sort | limited dna repair gene repertoire in ascomycete yeast revealed by comparative genomics |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145719/ https://www.ncbi.nlm.nih.gov/pubmed/31693105 http://dx.doi.org/10.1093/gbe/evz242 |
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